Abstract Reactions of unsaturated compounds with the PhSOEt-SOHal 2 and PhSOEt-Me 3 SiHal systems (Hal= Cl or Br) were proposed as a new route to haloalkyl phenyl sulfides. With acyclic and mono-and bicyclic alkenes and dienes as examples, the regio-and stereoselectivity of the reactions were studied.
[Watanabe, Mikio; Nakamori, Seijin; Hasegawa, Hatsue; Shirai, Kozo; Kumamoto, Takanobu Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 3 p. 817 - 821]
[Watanabe, Mikio; Nakamori, Seijin; Hasegawa, Hatsue; Shirai, Kozo; Kumamoto, Takanobu Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 3 p. 817 - 821]
